Limongelli G - Search Results

1

Fatal hypertrophic cardiomyopathy and nemaline myopathy associated with ACTA1 K336E mutation.

D'Amico A, Graziano C, Pacileo G, Petrini S, Nowak KJ, Boldrini R, Jacques A, Feng JJ, Porfirio B, Sewry CA, Santorelli FM, Limongelli G, Bertini E, Laing N, Marston SB. D'Amico A, et al. Among authors: limongelli g. Neuromuscul Disord. 2006 Oct;16(9-10):548-52. doi: 10.1016/j.nmd.2006.07.005. Epub 2006 Sep 1. Neuromuscul Disord. 2006. PMID: 16945537

2

Myocardial ultrasound tissue characterization in patients with hypertrophic cardiomyopathy: noninvasive evidence of electrical and textural substrate for ventricular arrhythmias.

Limongelli G, Pacileo G, Cerrato F, Verrengia M, Di Simone A, Severino S, Sarubbi B, Calabrò R. Limongelli G, et al. J Am Soc Echocardiogr. 2003 Aug;16(8):803-7. doi: 10.1067/S0894-7317(03)00213-X. J Am Soc Echocardiogr. 2003. PMID: 12878988

3

Familial aggregation of genetically heterogeneous hypertrophic cardiomyopathy: a boy with LEOPARD syndrome due to PTPN11 mutation and his nonsyndromic father lacking PTPN11 mutations.

Digilio MC, Pacileo G, Sarkozy A, Limongelli G, Conti E, Cerrato F, Marino B, Pizzuti A, Calabrò R, Dallapiccola B. Digilio MC, et al. Among authors: limongelli g. Birth Defects Res A Clin Mol Teratol. 2004 Feb;70(2):95-8. doi: 10.1002/bdra.10148. Birth Defects Res A Clin Mol Teratol. 2004. PMID: 14991917

4

Left ventricular hypertrophy in Caucasian master athletes: Differences with hypertension and hypertrophic cardiomyopathy.

Limongelli G, Verrengia M, Pacileo G, Da Ponte A, Brancaccio P, Canonico R, D'Andrea A, Sarubbi B, Cerasuolo F, Calabró R, Limongelli FM. Limongelli G, et al. Among authors: limongelli fm. Int J Cardiol. 2006 Jul 28;111(1):113-9. doi: 10.1016/j.ijcard.2005.07.033. Epub 2005 Nov 2. Int J Cardiol. 2006. PMID: 16260052

5

LEOPARD syndrome: clinical diagnosis in the first year of life.

Digilio MC, Sarkozy A, de Zorzi A, Pacileo G, Limongelli G, Mingarelli R, Calabrò R, Marino B, Dallapiccola B. Digilio MC, et al. Among authors: limongelli g. Am J Med Genet A. 2006 Apr 1;140(7):740-6. doi: 10.1002/ajmg.a.31156. Am J Med Genet A. 2006. PMID: 16523510

6

PTPN11 gene mutations: linking the Gln510Glu mutation to the "LEOPARD syndrome phenotype".

Digilio MC, Sarkozy A, Pacileo G, Limongelli G, Marino B, Dallapiccola B. Digilio MC, et al. Among authors: limongelli g. Eur J Pediatr. 2006 Nov;165(11):803-5. doi: 10.1007/s00431-006-0163-7. Epub 2006 May 30. Eur J Pediatr. 2006. PMID: 16733669

7

Noninvasive risk stratification prevents sudden death due to paroxysmal atrial fibrillation in hypertrophic cardiomyopathy.

Limongelli G, Elliott PM, Pacileo G, Sarubbi B, Thaman R, Calabrò P, Vergara P, Iacomino M, Russo MG, Calabrò R. Limongelli G, et al. J Cardiovasc Med (Hagerstown). 2006 Sep;7(9):711-3. doi: 10.2459/01.JCM.0000243007.97793.0f. J Cardiovasc Med (Hagerstown). 2006. PMID: 16932087

8

Myocardial infarction in a young athlete with non-obstructive hypertrophic cardiomyopathy and normal coronary arteries.

Limongelli G, Calabro' P, Pacileo G, Santoro G, Calabro' R. Limongelli G, et al. Int J Cardiol. 2007 Feb 7;115(2):e71-3. doi: 10.1016/j.ijcard.2006.07.206. Epub 2006 Oct 27. Int J Cardiol. 2007. PMID: 17069906

9

Is sudden cardiac death predictable in LEOPARD syndrome?

Limongelli G, Pacileo G, Calabrò R. Limongelli G, et al. Cardiol Young. 2006 Dec;16(6):599-601. doi: 10.1017/S1047951106001247. Cardiol Young. 2006. PMID: 17116277

10

Echocardiography in congenital heart disease: usefulness, limits and new techniques.

Pacileo G, Di Salvo G, Limongelli G, Miele T, Calabrò R. Pacileo G, et al. Among authors: limongelli g. J Cardiovasc Med (Hagerstown). 2007 Jan;8(1):17-22. doi: 10.2459/01.JCM.0000247430.36581.c2. J Cardiovasc Med (Hagerstown). 2007. PMID: 17255811 Review.

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